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Mechanism of H2 Evolution from a Photogenerated Hydridocobaloxime

Dempsey, Jillian L., Winkler, Jay R., Gray, Harry B.·2010·Journal of the American Chemical Society

Abstract

Proton transfer from the triplet excited state of brominated naphthol to a difluoroboryl bridged Co(I)-diglyoxime complex, forming Co(III)H, was monitored via transient absorption. The second-order rate constant for Co(III)H formation is in the range (3.5-4.7) × 10(9) M(-1) s(-1), with proton transfer coupled to excited-state deactivation of the photoacid. Co(III)H is subsequently reduced by excess Co(I)-diglyoxime in solution to produce Co(II)H (k(red) = 9.2 × 10(6) M(-1) s(-1)), which is then protonated to yield Co(II)-diglyoxime and H(2).

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Metadata

Authors
Dempsey, J. L., Winkler, J. R., & Gray, H. B.
Venue
Journal of the American Chemical Society
Published
2010-11-10
Volume
132
Issue
47
Pages
16774-16776
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2048813202
Cited by
225
References
0
FWCI
14.86
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Mechanism of H2 Evolution from a Photogenerated Hydridocobaloxime. https://app.cochat.ai/papers/10.1021/ja109351h
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Dempsey, J. L., Winkler, J. R., & Gray, H. B. (2010). Mechanism of H2 Evolution from a Photogenerated Hydridocobaloxime. Journal of the American Chemical Society. https://doi.org/10.1021/ja109351h

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.